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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2023. (Total: 223640Documents)
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Query Trace: Neuromuscular Diseases and CLCN1[original query]
In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia.
European journal of human genetics : EJHG 2008 Aug 16 (8): 921-9.
Trip Jeroen, Drost Gea, Verbove Dennis J, van der Kooi Anneke J, Kuks Jan B M, Notermans Nicolette C, Verschuuren Jan J, de Visser Marianne, van Engelen Baziel G M, Faber Carin G, Ginjaar Ieke
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